Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.

Patents

  1. Advanced Patent Search
Publication numberUS3779732 A
Publication typeGrant
Publication dateDec 18, 1973
Filing dateApr 16, 1971
Priority dateDec 11, 1969
Also published asUS3687799
Publication numberUS 3779732 A, US 3779732A, US-A-3779732, US3779732 A, US3779732A
InventorsSpanoudis L
Original AssigneeOwens Illinois Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method of making glass lasers of increased heat dissipation capability
US 3779732 A
Abstract  available in
Images(6)
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

United States Patent 1191 Spanoudis 1*Dec. 18, 1973 METHOD OF MAKING GLASS LASERS OF INCREASED HEAT DISSIPATION CAPABILITY [75] Inventor: Louis Spanoudis, Toledo, Ohio [73] Assignee: Owens-Illinois, Inc., Toledo, Ohio Notice: The portion of the term of this patent subsequent to May 2, 1989, has been disclaimed.

22 Filed: Apr. 16, 1971 211 Appl. No.: 134,892

Related US. Application Data [62] Division of Ser. No. 884,358, Dec. 11, 1969, Pat. No.

Primary Examiner-Arthur D. Kellogg Altomey-Richard D. Heberling et al.

[57] ABSTRACT Glass lasers containing at least 1 mole percent of lithium oxide based on the total glass composition expressed in oxide content and having a compressive stress surface layer whereby increased strength and increased heat dissipation capability is obtained. The compressive stress surface layer has essentially the same composition as the remainder of the glass laser except that the concentration of lithium ions is less than the remainder of said glass laser, and the concentration of ions of a different alkali metal is greater than the remainder of the glass laser. Laser glasses are generally first acid washed and then contacted with a salt of an alkali metal other than lithium at an elevated temperature and for a sufficient period of time to replace a portion of the lithium ions in the surface of the glass laser with the ions of the different alkali metal and thereby form the compressive stress layer in the surface, but for a time insufficient to produce any substantial relaxation of the stress formed in the surface layer. As a result of this treatment there is developed on the surface of the glass laser a thin surface layer of low order tension and a thicker underlayer of high compressive stress. The tension surface layer is then removed by acid wash to expose the compression layer.

14 Claims, N0 Drawings METHOD OF MAKING GLASS LASERS OF INCREASED HEAT DISSIPATION CAPABILITY The present application is a divisional of application Ser. No. 884,358, filed Dec. ll, 1969, now US. Pat. No. 3,687,799, issued Aug. 29, 1972.

Glass lasers designed for high energy applications are exposed to great amounts of heat. When a glass laser rod is pumped at high energy levels the major energy fraction is heat which is absorbed by the rod causing it to become hot.'Under prolonged conditions of operation, heating of the glass rod causes considerable distortion. In order to prevent distortion some methods in the prior art have resorted to water cooling of the rod. However, cooling of therod in this manner has not been altogether successful because the outside surface of the rod tends to go into tension. Longitudinal cracks have resulted in rods treated in this way and have rendered the glass rods useless for laser purposes. A common problem in the glass laser field is the particular damage which occurs when a heavily pumped glass laser is fired a number of times in rather rapid succession. Owing to the heat absorbed by the glass laser rod, a thermal gradient is set up and produces a stress condition whereby the center of the rod is under compression and the surface in tension. When the thermal gradient reaches such a magnitude that the tensile stress at the rod surface exceeds the rupture strength of the glass, the rod fractures. The damaged rod may exhibit either a lacework pattern of cracks or a single crack tending to split the rod lengthwise.

There is an upper limit to the magnitude of the thermal gradient that a laser rod can sustain and still retain its integrity. This thermal gradient merely reflects the rate at which heat is removed from the rod; i.e., heat must be removed at a rate which equals or exceeds the rate at which it is applied.

It is clear that the maximum sustainable thermal gradient determines the maximum average power'at which the laser rod can be safely irradiated. In other words, the maximum power handling capability of a laser rod is determined by that point at which the thermally induced tensile stress at the surface exceeds its rupture strength. For typical laser rods, this maximum power handling capability is relatively independent of the diameter of the rod and can be described in terms of a power loading per unit length.

The power loading referred to is the heat abosrbed by the laser rod when irradiated by the flash lamp and usually represents between percent and 25 percent of the flash lamp electrical input. For example, a laser rod being pumped over six inches of its length will withstand, without breaking, a maximum electrical input of about 1,200 watts or 200 watts per inch. This figure corresponds to an absorbed power of about 300 watts or 50 watts per inch.

The power loading capability or breakage point of a laser rod can be improved to a limited extent by using certain geometric configurations. For example, a hollow rod or tube can have a higher breakage point than a solid rod by a factor of two or three and still retain a reasonable efficiency. Aside from the doughnutshaped beam produced by tubes, this shape has other drawbacks, however. For example, the inner and outer surfaces must be cooled equally to gain full benefit, and usually this can only be accomplished by allowing the coolant to flow over the rod face. Such cooling causes the problems referred to above, namely, the outside surface of the rod tends to go into tension and as a result longitudinal cracks may form in the rod.

A much greater improvement in the average power handling capability of glass laser rods is therefore desired to accurately challenge the capabilities of flash lamps. In order to achieve that capability the glass laser rods resistance to breakage should be improved by a substantial factor, for example, at least four or five.

Several methods have been proposed for increasing the strength of glass laser rods. The approaches of decreasing the thermal expansion or increasing the thermal conductivity involves changing the composition of the glasses. In the case where the composition of the glass laser is highly important or critical for achieving certain beneficial results it is undesirable to modify the glass composition in any way.

It has now been determined that a significant improvement in the power handling capability of glass laser rods can be obtained and that the rods resistance to mechanical abuse can be significantly improved without changing the composition of the glass. This is accomplished in accordance with the present invention by forming a surface compressive layer in the glass laser component whereby increased strength and increased heat dissipation capability can be achieved.

Accordingly, it is an object of the present invention to provide glass laser components of increased heat dissipation capability and glass laser components of greater strength which overcome the problems that have been associated with prior glass lasers.

It is a further object of the present invention to provide a method for increasing the strength of glass laser rods.

It is a still further object of the present invention to provide a method of improving glass laser rods so that the glass laser rods can withstand high energy loading and perform satisfactorily.

In attaining the above objects, one feature of the present invention resides in a glass laser component which has formed in the surface thereof a compressive stress layer.

A further feature of this invention resides in improved glass lasers containing at least 1 mole percent lithium oxide based on the total glass composition expressed in oxide content having a surface compressive stress layer which is essentially the same composition as the remainder of the glass laser except that the concentration of lithium ions is less in the surface compressive stress layer than in the remainder of the glass laser and wherein the concentration of ions of a different alkali metal is greater in the compressive stress layer than in the remainder of the glass laser.

According to a further feature of the present invention, the glass laser rod containing at least 1 mole percent lithium is acid treated with an etching agent to remove at least a portion of the surface defects and/or flaws. The acid treated rod is then chemically tempered by contacting the glass laser rod with a salt of a different alkali metal at an elevated temperature for a sufficient period of time to exchange a portion of the lithium ion in the surface of the glass laser for the ions of the different alkali metal in contact with the glass surface. When glass lasers of high lithium oxide content; e.g., 20 mole percent are treated, a shallow, low order tension stress generally forms on the surface with a high compression layer underneath. The final step in the process is an acid wash to remove the thin tension layer on the surface and expose the underlying compressive stress layer.

The foregoing as well as other objects, features and advantages of the present invention will become apparent to those skilled in the art from the following detailed description of the invention.

Glass lasers for high energy application containing considerable amounts of lithium oxide have been disclosed in the art. For example, Lee et al, US. Pat. No. 3,471,409 discloses lithia silicate laser glasses containing at least 15 mole percent lighium oxide and which are highly efficient. The laseable substance contained in these glass lasers is neodymium oxide. In accordance with the present invention, glass lasers containing lithium oxide can be even further improved to remarkably improve their strength characteristics. Glass laser components containing at least 1 mole percent lithium oxide based on the total glass composition expressed in oxide content and containing a suitable laseable substance such as a rare earth oxide, e.g., neodymium oxide, can be treated in the following manner to form a compressive stress layer in the surfaces thereof.

In general, it has been found that the glass laser rod should first be contacted with an acid etching agent such as hydrofluoric acid to remove at least a portion, preferably substantially all, the surface imperfections, defects, flaws, which deleteriously affect the strength of the laser rod. An aqueous solution of hydrofluoric acid, either alone or mixed with other suitable materials known in the art, can be conveniently used for this purpose. The temperature of the etching bath can vary although ambient conditions or room temperature is sufficient for this purpose. The time of immersion, again, can vary widely from about 2 seconds to several minutes depending on the size and configuration of the laser as well as other factors. The hydrofluoric acid concentration in the etching bath is not narrowly critical and the generally well known hydrofluoric acid etching baths can be used for purposes of this invention, e.g., containing 38.8 percent by weight hydrofluoric acid. It is preferable to wash the acid from the rod after the immersion and this can be conveniently accomplished by rinsing in warm water. The acid immersion or acid washing procedure can be repeated several times in order to achieve adequate etching.

Following the acid etching step, the glass laser is immersed or otherwise contacted with a salt of a different alkali metal. The term different alkali metal as used herein means sodium, potassium, rubidium and cesium. For purposes of this invention, salts of sodium and potassium are preferred, with salts of sodium being most preferred. The salt of a different alkali metal can be in the form of a molten salt bath or can be used in an aqueous solution or organic solvent solution or in water and organic solvent mixtures. Sprays, mists and any other convenient method can be used for application of the salt to the glass laser rod. A molten bath of sodium nitrate at an elevated temperature of, for example, 350 C (662 F) has been found to be particularly satisfactory. The period of time can range from 5 minutes to 50 hours. The glass laser treated in this manner generally develops a combination surface layer that ranges from 5 to microns deep of low order tension with an underlayer of high compression which ranges from at least about 10, preferably 50 to 100 microns thick.

The third step of the process involves removal of the tension layer that is formed in the second step. The glass removal rate in the initial acid washing or fortification procedure of the first step can be calculated and then the required duration of the final acid wash can be calculated to remove an average tension layer. Thus, if the glass removal rate is 1.25 microns persecond, then an acid dip of 4 seconds each for a total of 12 seconds would be sufficient to remove an average tension layer. In an actual test cross-sectioning of the samples revealed that in fact the tension surface layer was removed.

It has also been determined that with glasses having a relatively low or no lithium content there is a minimum, if any, problem of tensile stress formation in the glass rod. Hence, the problem of the low order tension layer does not occur except in the area of high lithium containing laser glasses. Consequently, the final acid wash may not be necessary to obtain a useful product.

In forming a glass laser rod, the molten glass composition made from the usual glass forming batch ingredients is first cast as a billet using conventional or available techniques. The glass billet can be formed into a suitable rod by a grinding technique such as a centerless grinder. These procedures leave a relatively rough surface layer on the rod having many surface imperfections which considerably reduces the strength of the rod. Therefore, the initial acid etching step is usually desirable.

In carrying out the present invention any molten alkali metal salt, other than a lithium salt, can be used which does not decompose at the temperatures employed providing it is capable of disassociating so that it frees the alakli metal ion for ion exchange in replacing the lithium ion in the surface of the glass rod. Generally, temperatures below the strain point of the glass are preferred, particularly from 50 to C below the strain point, although this can be varied. The temperature for the ion exchange is usually at least 200 C and less than the fiber softening point of the glass. The elevated temperature and the duration of the ion exchange step should be insufficient to relax the compressive stress formed in the surface layer of the glass laser.

Thus, sodium salts such as sodium sulfate, sodium nitrate, sodium chloride, sodium fluoride and soduim phosphate can be used for purposes of the present invention. Generally, the molten alkali metal salt is placed in a suitable crucible such as a platinum crucible or preferably a ceramic crucible to prevent any metallic ions from being introduced into the molten salt bath which might interfere with the ion exchange. The size of the crucibles can vary depending upon the nature of the ion exchange reactions that take place. If small laser rods are ion exchanged then the crucible can be relatively small.

As used in the present application the expression lithium containing glasses" are those lithium-alumina silicate glasses which contain at least about 1 mole percent generally at least about 15 mole percent lithium oxide, Li O. The following are representative lithiasilicate glass lasers suitable for practice of this invention. In these compositions, neodymium oxide, Nd o is the laseable substance, however, any suitable and compatible laseable material such as a rare earth oxide can be used in place of the neodymium oxide.

Lithia-silicate glasses containing the following ingredients in the approximate mole percent:

SiO -45 to 75 Al O to 8 Li Ol to 35 CaO0.5 to 30 Preferred compositions are shown below in mole percent:

SiO 48 to 65 Al O 0 to 8 Li O20 to 30 CaO5 to 25 CeO 0.l to 0.3

Nd O 0.01 to 2 Optimum compositions are shown below in mole percent:

SiO 49 to 62 Al O --2 to 5 Li O-25 to 30 Ca08 to 22 CeO -0.1 to 0.2

There are many advantages apart from increased power capability to be gained from the use of strengthened glass laser rods. For example, strengthened rods are more resistant to damage resulting from careless handling. Typically, a normal 1/4 inch X 3 inch glass laser rod will shatter after a 4 foot drop onto the floor. A rod that has been treated and accordingly strengthened by following the procedures described in this application will usually bounce and suffer only an occasional chipping of the edge. It is expected that strengthened laser rod faces will be more resistant to damage from exploding dust particles and the like. Initial observations indicate that the strengthened faces do not interfere with lasing action.

It has been determined that under the preferred conditions of the present invention the glass laser rod having the high lithia content is acid polished with a solution of 60 volume percent of 48 percent hydrofluoric acid and 40 volume percent water. Multiple short clips are preferred over a longer, single dip. An intermediate rinse in concentrated sulfuric acid is preferably employed. During the rinse, an effervescence occurred which facilitates removal of the fluorides formed in the HF bath. It has been calculated that this treatment is capable of removing 1.25 microns per second when dips in the mixed acid bath were 5 seconds in duration.

When using a sodium salt for the ion exchange process, for example, the formation of the compressive layer on a high lithium glass laser rod is in accordance with the simple sodium-for-lithium ion exchange and follows the diffusion laws. Lower treatment temperatures give lower depths while higher treatment temperatures give greater depths but much less compressive stress and thicker tension layers on the surface. The tension layer on the surface varies with the time of treatment and is extremely difficult to measure. Typical measurements are shown in the following Table 1 wherein the laser glass had the same composition as shown in Example I:

TABLE l.-TENSlON SURFACE LAYER ON GLASS OF EXAMPLE 1 After ion exchange it was found that an acid etching process is effective in removing the tension layer on the surface. The same type of hydrofluoric acid solution is suitable for this purpose. Knowing the thickness of the tension layer formed and the glass removal rate in the acid it was possible to calculate the acid treatment. For example: in a 48 hour ion exchange conducted at 350 C. using sodium nitrate, a tension layer of about 20 microns thick was formed. Since the etch rate is 1.25 microns per second then the total etch time would be 20/1.25 or 16 seconds. This means that approximately three 5 second acid dips would remove the tension layer formed in the first step.

Rods treated for a total of 135 hours in sodium nitrate at 662 F. with intermediate acid treatments of hydrofluoric acid to remove the tension layer on the surface have an average abraded modulus of rupture of about 40,000 psi with a standard deviation of 16,000 psi. This compared very favorably with untreated abraded rods which had an average modulus of rupture of 6,800 psi and a standard deviation of 375 psi.

The abrasion technique was to place 5 rods in a 1 gallon plastic jar with 1,000 grams of No. 46 grit silicon carbide and rotating on a ball mill rack for 15 minutes. The modulus or rupture testing was done with standard four-point loading. Cross-sectioning of the strengthened rods revealed a stress of approximately 41,000 psi at a depth of about microns.

The following example illustrates the present invention:

EXAMPLE I A sample of the following glass laser l/4 inch diame' ter by 6 inches long was used in this test:

Weight Percent The glass laser rod was acid fortified by immersing in an aqueous solution of hydrofluoric acid at room temperature for 5 seconds. The hydrofluoric acid concentration was 38.8 percent by weight. After washing in the acid the rod was rinsed in warm tap water. This procedure was repeated 11 more times for a total of 12 times.

The rod was then immersed in a molten bath of sodium nitrate at 350 C (662 F) for 48 hours.

Samples treated showed a surface layer 15 microns deep of low order tension with an underlayer of 38,000 psi compression which was microns thick.

The glass laser rod was then dipped three times for four seconds each for a total of 12 seconds to remove the tension layer that was formed. This was calculated on the basis that the glass removal rate using the acid wash or fortification procedure of Step 1 was 1.25 microns per second. A cross-section revealed in fact, that the tension surface layer had been removed.

Glass laser rods treated as described above were tested in a standard modulus of rupture test with a 4 inch support span and a 3/4 inch load span. The following results were obtained:

The silicon carbide abuse was administered by placing the rods in a 1 gallon wide mouth polyethylene jar with 1,000 grams of 46 grit silicon carbide and rotating minutes on a ball mill rack.

The glass-to-glass abuse was identical except that there was no silicon carbide.

Using the process described in the present application the high reflectivity, high lithia containing laser glasses are not deleteriously affected. Furthermore, the glasses of the present invention have a beam divergence of only 1.5 milliradians which is due primarily to the high efficiency of the high lithium containing laser glasses combined with its higher thermal conductivity. Over 120,000 shots were made during the testing of this laser with no output degradation detected due to deterioration of the laser rod.

Usually a glass laser rod will not survive large thermal loadings because of its relatively low coefficient to thermal conductivity and relatively high coefficient to thermal expansion. At high thermal loadings, hoop stresses exceed the strength of the material and cause the rod to break. The present invention overcomes these problems and improves the utility of glass laser rods by increasing enormously the strength of the glass laser rods having a high lithia content. A comparative test conducted between an identical laser rod having the identical chemical composition and one strengthened in accordance with the present invention reveals that the unstrengthened glass laser rod fractured at power loadings of approximately 80 watts per centimeter. This figure corresponds to an average power output from the laser rod of approximately 10 watts. The strengthened rod, however, did not break and was still operating satisfactorily at more than watts output. With extreme loadings applied, the strengthened rod withstood power loadings without breakage up to 400 watts per centimeter. Thus, the present invention provides a method for remarkably improving the strength of glass lasers containing at least 1 mole percent lithium oxide.

It is understood that various other modifications will be apparent to and can readily be made by those skilled in the art without departing from the scope and spirit of this invention. Accordingly, it is not intended that the scope of the claims appended hereto be limited to the description set forth herein but rather that the claims be construed as encompassing all the features of patentable novelty which reside in the present invention including all features which would be treated as equivalents thereof by those skilled in the art to which the invention pertains.

What is claimed is:

l. A method for strengthening a silicate glass laser containing at least about 1 mole percent of lithium oxide based on the total glass composition expressed as oxide content comprising:

contacting a surface of said glass laser with an acidic etching agent to remove at least a portion of the surface defects and flaws of said surface,

thereafter applying to said surface an ion exchange salt consisting of a salt of a different alkali metal and subjecting the glass in contact with said salt of said different alkali metal to elevated temperature for a sufficient period of time to exchange at least a portion of the lithium ions in said surface for the ions of said different alkali metal in contact with the surface of the glass laser and thereby develop a compressive stress layer in the glass layer, but for a time insufficient to relax the stress produced in the surface of the glass laser, the exchange of ions being capable of producing a tension surface layer over the compressive stress layer; and

thereafter treating said surface with an acidic etching agent of sufficient acid strength and for a sufficient period of time to remove the tension surface layer formed thereon.

2. The method as set forth in claim 1 wherein said elevated temperature is below the strain point of the glass laser.

3. The method as set forth in claim 2 wherein the elevated temperature is within the range of 50 to 100 C below the strain point of the glass laser.

4. The method as set forth in claim 1 wherein the different alkali metal is sodium.

5. The method as set forth in claim 1 wherein the salt of a different alkali metal is a member selected from the group consisting of sodium sulfate, sodium nitrate, sodium chloride, sodium fluoride and sodium phosphate.

6. The method as set forth in claim 1 wherein the glass laser has a content of lithium oxide of at least 5 mole percent.

7. The method as set forth in claim 1 wherein the salt of a different alkali metal is sodium nitrate.

8. The method as set forth in claim 1 wherein the salt of a different alkali metal is in molten form.

9. The method as set forth in claim 1 wherein the glass laser contains the following ingredients in the approximate mole percent:

SiO 45 to 75 Al O 0 to 8 Li Ol5 to 35 CaO0.5 to 30 10. The method as set forth in claim 1 wherein the glass laser contains the following ingredients in the approximate mole percent:

SiO 48 to AlgOg-O t0 8 11 0-20 to 30 CaO-5 to 25 CeO 0.1 to 0.3

11. A method for strengthening a silicate glass laser containing at least about 1 mole percent lithium oxide based on the total glass composition expressed as oxide content comprising:

applying to at least one surface of said glass laser an acidic etching agent to remove at least a portion of the surface defects and flaws of said surface;

thereafter applying to said at least one surface, an ion exchange salt consisting of a salt of a different alkali metal and subjecting the glass laser in contact with said salt to elevated temperature below the strain point of the glass laser for a sufficient period of time to exchange at least a portion of the lithium ions in said surface for the ions of said different alkali metal in contact with the surface of the glass and thereby develop a compressive stress layer in the glass laser, but for a time insufficient to relax the stress produced in the surface of the glass laser, the exchange of ions being capable of producing a tension surface layer over the compressive layer,

and thereafter treating said surface with an acidic etching agent of sufficient acid strength and for a sufficient period of time to remove the tension surface layer formed thereon.

12. A method as set forth in claim 1 1 wherein said elevated temperature is below the strain point of the glass.

13. A method for strengthening a shaped silicate glass laser article containing at least about 1 mole percent lithium oxide based on the total glass composition expressed as oxide content comprising:

applying to at least one surface of the laser an acidic etching agent comprising hydrofluoric acid to remove at least a portion of the surface defects and flaws of said surface,

thereafter washing the laser and contacting said at least one surface with an ion exchange salt consisting of a molten salt of sodium at an elevated temperature below the strain point of the glass for a sufficient period of time to exchange at least a portion of the lithium ions in said surface with the so dium ions of said salt in contact with said surface, and thereby develop a compressive stress layer in the glass laser, but for a time insufficient to relax the stress produced in the surface of the glass laser, the exchange of ions being capable of producing a tension surface layer over the compressive layer,

and thereafter washing said at least one surface with hydrofluoric acid of sufficient strength and for a sufficient period of time to remove a tension layer formed in said at least one surface.

14. A method for strengthening silicate glass lasers containing at least about 1 mole percent of lithium oxide based on the total glass composition expressed as oxide content comprising:

contacting a surface of said glass laser with an acidic etching agent to remove at least a portion of the surface defects and flaws of said surface,

contacting at least one surface of said glass laser with an ion exchange salt consisting of a salt of a different alkali metal and subjecting the glass in contact with said salt of said different alkali metal to elevated temperature for a sufficient period of time to exchange at least a portion of said lithium ions in the surface of said glass laser for the ions of said different alkali metal in contact with the surface of the glass and thereby develop a compressive stress layer in the glass, but for a time insufficient to relax the stress produced in said surface of the glass la-

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US3023139 *Mar 11, 1958Feb 27, 1962Floris Van Tetterode And Jan DMethod of strengthening sheet glass in agitated liquid fluoride bath
US3357876 *Jan 19, 1965Dec 12, 1967Pittsburgh Plate Glass CoMethod of strengthening a glass article by ion exchange
US3484224 *May 13, 1966Dec 16, 1969Ici LtdMethod of chemically strengthening glass
US3535266 *Apr 25, 1966Oct 20, 1970Owens Illinois IncGlass laser compositions
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3982917 *Feb 4, 1975Sep 28, 1976The United States Of America As Represented By The Secretary Of The ArmyMethod of increasing the strength of silicate glass laser rods
US3997312 *Apr 2, 1975Dec 14, 1976U.S. Philips CorporationMethod of manufacturing colored glass articles
US4130407 *Jun 16, 1977Dec 19, 1978Duraglass Research & Development Corp.Strengthening of glass
US5674790 *Dec 15, 1995Oct 7, 1997Corning IncorporatedStrengthening glass by ion exchange
US5908716 *Apr 15, 1997Jun 1, 1999Valence Technology, Inc.Lithium--containing sulfates, method of preparation and uses thereof
US8889254Jan 7, 2011Nov 18, 2014Corning IncorporatedImpact-damage-resistant glass sheet
US8978414Nov 9, 2012Mar 17, 2015Corning IncorporatedAcid strengthening of glass
US9346707Nov 25, 2013May 24, 2016Corning IncorporatedMethods for forming delamination resistant glass containers
US9428302Oct 18, 2013Aug 30, 2016Corning IncorporatedDelamination resistant glass containers with heat-tolerant coatings
US9505653Dec 30, 2014Nov 29, 2016Corning IncorporatedAcid strengthening of glass
US20060177664 *Sep 13, 2005Aug 10, 2006Takashi NaitouGlass member
US20070029925 *Oct 13, 2006Feb 8, 2007Takashi NaitouGlass member
US20110165393 *Jan 7, 2011Jul 7, 2011John Frederick BayneImpact-damage-resistant glass sheet
CN102741187A *Jan 7, 2011Oct 17, 2012康宁股份有限公司Impact-damage-resistant glass sheet
CN102741187B *Jan 7, 2011Sep 9, 2015康宁股份有限公司抗冲击损伤玻璃片
WO2011085190A1 *Jan 7, 2011Jul 14, 2011Corning IncorporatedImpact-damage-resistant glass sheet
WO2016037083A1 *Sep 4, 2015Mar 10, 2016Corning IncorporatedGlass articles and methods for improving the reliability of glass articles
Classifications
U.S. Classification65/31, 65/30.13, 65/116
International ClassificationC03C4/00, H01S3/17, C03C21/00, H01S3/08, C03C15/00
Cooperative ClassificationH01S3/17, H01S3/08072, C03C15/00, C03C21/002, C03C4/0071
European ClassificationC03C15/00, C03C21/00B2, C03C4/00N, H01S3/17
Legal Events
DateCodeEventDescription
Sep 17, 1980AS02Assignment of assignor's interest
Owner name: OWENS-ILLINOIS, INC.
Owner name: SCHOTT OPTICAL GLASS, INC., YORK AVE.,DURYEA,PA,18
Effective date: 19800711